4.6 Article

MetabolitePredict: A de novo human metabolomics prediction system and its applications in rheumatoid arthritis

期刊

JOURNAL OF BIOMEDICAL INFORMATICS
卷 71, 期 -, 页码 222-228

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jbi.2017.06.002

关键词

Human metabolomics; Metabolomic biomarker discovery; Human gut microbiome; Metaboloite inhibitor; Rheumatoid arthritis

资金

  1. Eunice Kennedy Shriver National Institute Of Child Health & Human Development of the National Institutes of Health under NIH [DP2HD084068]
  2. Case Western Reserve University/Cleveland Clinic CTSA [UL1TR000,439]
  3. American Cancer Society [RSG-16-049-01-MPC]
  4. Landon Foundation-AACR INNOVATOR for Cancer Prevention Research [15-20-27-XU]
  5. Pfizer Investigator Initiated Research Grant [WI206753]

向作者/读者索取更多资源

Human metabolomics has great potential in disease mechanism understanding, early diagnosis, and therapy. Existing metabolomics studies are often based on profiling patient biofluids and tissue samples and are difficult owing to the challenges of sample collection and data processing. Here, we report an alternative approach and developed a computation-based prediction system, MetabolitePredict, for disease metabolomics biomarker prediction. We applied MetabolitePredict to identify metabolite biomarkers and metabolite targeting therapies for rheumatoid arthritis (RA), a last-lasting complex disease with multiple genetic and environmental factors involved. MetabolitePredict is a de novo prediction system. It first constructs a disease-specific genetic profile using genes and pathways data associated with an input disease. It then constructs genetic profiles for a total of 259,170 chemicals/metabolites using known chemical genetics and human metabolomic data. MetabolitePredict prioritizes metabolites for a given disease based on the genetic profile similarities between disease and metabolites. We evaluated MetabolitePredict using 63 known RA-associated metabolites. MetabolitePredict found 24 of the 63 metabolites (recall: 0.38) and ranked them highly (mean ranking: top 4.13%, median ranking: top 1.10%, P-value: 5.08E-19). MetabolitePredict performed better than an existing metabolite prediction system, PROFANCY, in predicting RA-associated metabolites (PROFANCY: recall: 0.31, mean ranking: 20.91%, median ranking: 16.47%, P-value: 3.78E-7). Short-chain fatty acids (SCFAs), the abundant metabolites of gut microbiota in the fermentation of fiber, ranked highly (butyrate, 0.03%; acetate, 0.05%; propionate, 0.38%). Finally, we established MetabolitePredict's potential in novel metabolite targeting for disease treatment: MetabolitePredict ranked highly three known metabolite inhibitors for RA treatments (methotrexate:0.25%; leflunomide: 0.56%; sulfasalazine: 0.92%). MetabolitePredict is a generalizable disease metabolite prediction system. The only required input to the system is a disease name or a set of disease-associated genes. The web-based MetabolitePredict is available at: http://xulab.case.edu/MetabolitePredict. (C) 2017 Elsevier Inc. All rights reserved.

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